Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,619 recalls have been distributed to New York in the last 12 months.
Showing 35481–35500 of 55,896 recalls
Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...
The Issue: Possible contamination of product with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wegmans Milk Chocolate Covered Pretzels Recalled by First Source, LLC Due to...
The Issue: Milk Chocolate covered pretzels have incorrect rear label. The rear label is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ashby's Sterling Peanut Butter Landslide Ice Cream Recalled by House Of...
The Issue: House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViaPeel PTFE Peelable Introducer 5FR Recalled by Greatbatch Medical Due to...
The Issue: Greatbatch received complaints with the ViaPeel Introducer Sheath 5FR, of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Recalled by Medtronic Inc Due to Medtronic identified an issue with...
The Issue: Medtronic identified an issue with specific models and lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elana Surgical KitHUD The Elana Surgical KitHUD Recalled by Elana, Inc. Due...
The Issue: Elana has issued this Field Action to voluntarily remove specific serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...
The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...
The Issue: A review of packaging revealed the seal integrity of the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.